Canonical Allele Identifier: CA463853054
Gene: KCNV2 HGNC NCBI

Linked Data

dbSNP Id: rs1417069678
gnomAD v4: 9-2717970-G-A
MyVariant Identifiers: chr9:g.2717970G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717970G>A , CM000671.2:g.2717970G>A GRCh38
NC_000009.11:g.2717970G>A , CM000671.1:g.2717970G>A GRCh37
NC_000009.10:g.2707970G>A NCBI36
NG_012181.1:g.5445G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.231G>A MANE Select ENSP00000371514.3:p.Gln77=
ENST00000382082.3:c.231G>A ENSP00000371514.3:p.Gln77=
NM_133497.3:c.231G>A NP_598004.1:p.Gln77=
XR_929202.1:n.732G>A
XR_929203.1:n.732G>A
NM_133497.4:c.231G>A MANE Select NP_598004.1:p.Gln77=